Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:131425070-131425286 | Common:7; Rare:40 | ||||
chr2:131542335-131542478 | Rare:27 | ||||
chr2:131682408-131682552 | Common:3; Rare:48 | ||||
chr2:133266202-133266368 | Common:1; Rare:31 | ||||
chr2:135162815-135163086 | Common:1; Rare:72; Clinvar (benign):4 | ||||
chr2:135522420-135522656 | Rare:47 | ||||
chr2:135761678-135761908 | Rare:58 | ||||
chr2:137684890-137685040 | Common:3; Rare:34 | ||||
chr2:137688238-137688512 | Common:2; Rare:62 | ||||
chr2:138567491-138567759 | Rare:44 | ||||
chr2:138780876-138780911 | Rare:7 | ||||
chr2:140427515-140427779 | Common:1; Rare:50 | ||||
chr2:142492174-142492247 | Rare:11 | ||||
chr2:148933116-148933402 | Rare:34 | ||||
chr2:151339315-151339479 | Common:1; Rare:30 |